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Sodium Methoxide → 4-Benzyl-2-(methylsulfanyl)-3-nitro-1H-pyrrole

HRID 1979735
ノート
印刷プレビュー

反応式

HRID 1979735 の反応式
C[O-].[Na+].Cl.[NH2:5][CH2:6][C:7](=O)[CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[N+:16]([CH:19]=[C:20](SC)[S:21]([CH3:23])=O)([O-:18])=[O:17]>CO>[CH3:23][S:21][C:20]1[NH:5][CH:6]=[C:7]([CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:19]=1[N+:16]([O-:18])=[O:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 10942334Sodium MethoxideHCID 132906721-Amino-3-phenylpropan-2-one--hydrogen chloride (1/1)HCID 544870941-Nitro2-methylthio-2-methylsulphinylethylene

生成物 1

HCID 136466304-Benzyl-2-(methylsulfanyl)-3-nitro-1H-pyrrole収率 28.5%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

A solution of sodium methoxide (sodium (1.9 g, 0.084 mol) dissolved in methanol (100 ml)) and a solution of 1-amino-3-phenylpropan-2-one hydrochloride (7.9 g, 0.042 mol) in methanol (100 ml) were simultaneously added dropwise, to a stirred solution of 1-nitro-2-methylthio-2-methylsulphinylethylene (7.7 g, 0.042 mol) in methanol. The temperature was maintained at about 60° during the addition, which took 25 minutes. The solvent was then removed in vacuo, and the residual dark red oil was chromatographed on a silica gel column. Elution and recrystallisation with petroleum ether/ethyl acetate (7:3) gave 2-methylthio-3-nitro-4-benzylpyrrole (2.95 g, 28.5%) m.p. 190°-192.5°.

後処理

  1. temperatureThe temperature was maintained at about 60° during the addition, which
  2. customThe solvent was then removed in vacuo
  3. customthe residual dark red oil was chromatographed on a silica gel column
  4. washElution and recrystallisation with petroleum ether/ethyl acetate (7:3)

出典と根拠

ORDレコード
ord-04f2ce2c90214b21a2f27b76363aa583
出典データセット
uspto-grants-1984_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04482563

反応ノート

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